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| Job Location | Pune |
| Education | Not Mentioned |
| Salary | Rs 1.5 - 3.0 Lakh/Yr |
| Industry | Pharma / Biotech |
| Functional Area | Medical TranscriptionPharmacist / Medical Representative |
| EmploymentType | Full-time |
Job SummaryOverall responsibility for study management, responsible for the monitoring of studies in accordance with protocol/ SOPs/ Guidelines.Responsibilities and Duties- Perform Site Identification and conduct Feasibility Studies.- Perform Site Selection Visit, Site Initiation Visits in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines.- Send Follow Up letters to sites and submit Visit Reports to the Clinical Team Leader/ Project Manager as required.- Keep a close association with site (s) for Patient Recruitment, Patient Follow Up, and protocol-related activities.- Training of Investigators on Protocol and.- CRF retrieval as per the project instructions.- Coordinate and distribute Clinical Study Material to study sites.- Archival of study documents.Key SkillsBiotechnology, Microbiology, Upstream Downstream Processing Executive, Production Maintenance, Pharma, study documents, Central Clinical File, local regulatory guidelinesRequired Experience and QualificationsQualifications: Msc., life science, nursing , B.Pharmacy/M.Pharmacy/ PharmD, M.B.B.S, B.D.S, B.H.M.S, B.A.M.S, etc.) and life science graduates.Experience:FresherBenefitsPick n DropPF
Keyskills :
microbiology pharmacovigilance pharmacy linicalresearch lifesciences